J. M. Connor

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

Eileen M. Shore, Meiqi Xu, George Feldman et al. · Nature Genetics · 2006 · 1.2K citations

Recurrent Mutation, Fibrosis, Signal Transduction +11

EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

Alan Fryer, J. M. Connor, S. Povey et al. · The Lancet · 1987 · 514 citations

Cytogenetics, Genetic Disorder, Genetics +5

Early Pregnancy Levels of Pregnancy-Associated Plasma Protein A and the Risk of Intrauterine Growth Restriction, Premature Birth, Preeclampsia, and Stillbirth

Gordon C. S. Smith, Emily Stenhouse, Jennifer A. Crossley et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 466 citations

Fertility, Intrauterine Growth Restriction, Gynecology +16

Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1

Frederick S. Kaplan, Meiqi Xu, Petra Seemann et al. · Human Mutation · 2008 · 436 citations

Fibrodysplasia ossificans progressiva. The clinical features and natural history of 34 patients

J. M. Connor, DA Evans · Journal of Bone and Joint Surgery - British Volume · 1982 · 362 citations

Thumb Hypoplasia, Fibrosis, Medical Treatment +15